@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_head
{
this:
np:hasAssertion
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_assertion
;
np:hasProvenance
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_assertion
a
np:Assertion
.
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_provenance
a
np:Provenance
.
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_assertion
{
miriam-gene:89866
a
ncit:C16612
.
lld:C0750957
a
ncit:C7057
.
dgn-gda:DGN30e39976ea368c40343396558780bd5e
sio:SIO_000628
miriam-gene:89866
,
lld:C0750957
;
a
sio:SIO_001121
.
}
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_provenance
{
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_assertion
dcterms:description
"[RGPR was the first gene found to be mutated in XLRP, the subtype of RP displaying the most severe form of retinal degeneration with partial or complete blindness in the third or fourth decade of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:12402343
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP211438.RAIAmZwuK636t8O3hwZB73uPpFrkrI_qUcHsxcF8qpdGQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:56+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}